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JAG1 Gene Alagille Syndrome Type 1 Genetic Test

4,400 د.إ

-21%

The JAG1 Gene Alagille Syndrome Type 1 Genetic Test is a comprehensive diagnostic examination designed to detect mutations in the JAG1 gene, which are primarily associated with Alagille Syndrome Type 1. This condition is a genetic disorder that can affect multiple organ systems, including the liver, heart, skeleton, eyes, and kidneys. It is characterized by a variety of symptoms ranging from mild to severe, such as jaundice, heart defects, and characteristic facial features.

The test is carried out at DNA Labs UAE, a leading facility in genetic diagnostics, ensuring high-quality testing and accuracy. The cost of the test is 4400 AED, an investment towards a precise diagnosis that can significantly aid in managing the condition through early intervention and tailored treatment plans. This genetic test is crucial for families with a history of Alagille Syndrome or individuals showing symptoms related to the disorder, providing them with vital information for informed healthcare decisions.

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JAG1 Gene Alagille Syndrome Type 1 Genetic Test

Components: JAG1 Gene Alagille syndrome type 1 Genetic Test

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test Type: Dysmorphology

Doctor: Pediatrics

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for JAG1 Gene Alagille syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with JAG1 Gene Alagille syndrome type 1 NGS Genetic DNA Test gene JAG1

Test Details

The JAG1 gene is associated with a genetic disorder called Alagille syndrome type 1. Alagille syndrome is a rare genetic disorder that affects multiple systems in the body, including the liver, heart, and other organs.

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous analysis of multiple genes or even the entire genome. In the case of Alagille syndrome type 1, NGS can be used to identify mutations or variations in the JAG1 gene that may be responsible for the disorder.

NGS genetic testing for Alagille syndrome type 1 involves obtaining a DNA sample, usually through a blood sample or cheek swab, and then sequencing the JAG1 gene to look for any genetic changes. These changes may include small mutations, deletions, or duplications in the gene that can disrupt its normal function.

By identifying specific genetic changes in the JAG1 gene, NGS testing can help confirm a diagnosis of Alagille syndrome type 1 in individuals with suspected symptoms. It can also be used for carrier testing in family members of affected individuals or for prenatal testing in pregnancies at risk for the disorder.

It is important to note that genetic testing, including NGS, should always be done under the guidance of a healthcare professional or genetic counselor who can help interpret the results and provide appropriate counseling and support.

Test Name JAG1 Gene Alagille syndrome type 1 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for JAG1 Gene Alagille syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with JAG1 Gene Alagille syndrome type 1 NGS Genetic DNA Test gene JAG1
Test Details

The JAG1 gene is associated with a genetic disorder called Alagille syndrome type 1. Alagille syndrome is a rare genetic disorder that affects multiple systems in the body, including the liver, heart, and other organs.

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous analysis of multiple genes or even the entire genome. In the case of Alagille syndrome type 1, NGS can be used to identify mutations or variations in the JAG1 gene that may be responsible for the disorder.

NGS genetic testing for Alagille syndrome type 1 involves obtaining a DNA sample, usually through a blood sample or cheek swab, and then sequencing the JAG1 gene to look for any genetic changes. These changes may include small mutations, deletions, or duplications in the gene that can disrupt its normal function.

By identifying specific genetic changes in the JAG1 gene, NGS testing can help confirm a diagnosis of Alagille syndrome type 1 in individuals with suspected symptoms. It can also be used for carrier testing in family members of affected individuals or for prenatal testing in pregnancies at risk for the disorder.

It is important to note that genetic testing, including NGS, should always be done under the guidance of a healthcare professional or genetic counselor who can help interpret the results and provide appropriate counseling and support.